# Sutter Corp.

- Location (FDA's records): San Diego, CA
- FDA decisions: 7 (1989–1995): 7 510(k) clearances
- Product codes: BXB (5), KWH (1), KYJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Brm Extremities: 1 (https://510kreport.com/company/brm-extremities)

## Its most-cited devices
- K931588: Sutter Proximal Interphalangeal Joint (1994), cited by 1

## Recent decisions
- K943354: Sutter Hammertoe Joint Prosthesis (Jun 12, 1995)
- K945221: Sutter Model 6000 Hand CPM Device (Feb 27, 1995)
- K931588: Sutter Proximal Interphalangeal Joint (Mar 10, 1994)
- K924654: First Metatarsophalangeal Joint Motion Splint (Feb 22, 1993)
- K914860: Sutter Model 10000 Leg CPM Device (Jan 8, 1992)
- K902707: Model 9000 at Ankle CPM Device (Jul 25, 1990)
- K890607: Sutter Hospital CPM (Feb 27, 1989)

Source page: https://510kreport.com/company/sutter